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加拿大共识推荐意见:KRAS G12C 突变型 NSCLC 的管理

Canadian Consensus Recommendations on the Management of KRAS G12C-Mutated NSCLC.

机构信息

Division of Medical Oncology, William Osler Health System, University of Toronto, Brampton, ON L6R 3J7, Canada.

Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada.

出版信息

Curr Oncol. 2023 Jul 6;30(7):6473-6496. doi: 10.3390/curroncol30070476.

Abstract

Activating mutations in , in particular, a point mutation leading to a glycine-to-cysteine substitution at codon 12 (G12C), are among the most frequent genomic alterations in non-small cell lung cancer (NSCLC). Several agents targeting KRAS G12C have recently entered clinical development. Sotorasib, a first-in-class specific small molecule that irreversibly inhibits KRAS G12C, has since obtained Health Canada approval. The emergence of novel KRAS-targeted therapies warrants the development of evidence-based consensus recommendations to help clinicians better understand and contextualize the available data. A Canadian expert panel was convened to define the key clinical questions, review recent evidence, and discuss and agree on recommendations for the treatment of advanced -mutated NSCLC. The panel agreed that testing for KRAS G12C should be performed as part of a comprehensive panel that includes current standard-of-care biomarkers. Sotorasib, the only approved KRAS G12C inhibitor in Canada, is recommended for patients with advanced KRAS G12C-mutated NSCLC who progressed on guideline-recommended first-line standard of care for advanced NSCLC without driver alterations (immune-checkpoint inhibitor(s) [ICIs] +/- chemotherapy). Sotorasib could also be offered as second-line therapy to patients who progressed on ICI monotherapy that are not candidates for a platinum doublet and those that received first-line chemotherapy with a contraindication to ICIs. Preliminary data indicate the activity of KRAS G12C inhibitors in brain metastases; however, the evidence is insufficient to make specific recommendations. Regular liver function monitoring is recommended when patients are prescribed KRAS G12C inhibitors due to risk of hepatotoxicity.

摘要

在非小细胞肺癌 (NSCLC) 中,最常见的基因组改变之一是 中的激活突变,特别是导致密码子 12 处甘氨酸到半胱氨酸取代的点突变 (G12C)。最近,有几种针对 KRAS G12C 的药物进入了临床开发阶段。Sotorasib 是一种首创的特异性小分子药物,可不可逆地抑制 KRAS G12C,现已获得加拿大卫生部的批准。新型 KRAS 靶向疗法的出现需要制定基于证据的共识建议,以帮助临床医生更好地理解和理解现有数据。一个加拿大专家小组被召集来定义关键的临床问题,回顾最近的证据,并讨论和商定治疗晚期 KRAS 突变型 NSCLC 的建议。专家组一致认为,应将 KRAS G12C 检测作为包括当前标准护理生物标志物在内的综合检测的一部分。Sotorasib 是加拿大唯一批准的 KRAS G12C 抑制剂,推荐用于晚期 KRAS G12C 突变型 NSCLC 患者,这些患者在没有驱动基因突变的情况下,经指南推荐的一线标准治疗(免疫检查点抑制剂[ICI] +/- 化疗)进展。对于进展期 ICI 单药治疗且不符合铂类双联治疗条件的患者,以及接受一线化疗且对 ICI 有禁忌症的患者,也可以将 Sotorasib 作为二线治疗药物。初步数据表明 KRAS G12C 抑制剂在脑转移中的活性;然而,证据不足以做出具体建议。由于存在肝毒性风险,建议在患者开 KRAS G12C 抑制剂时定期进行肝功能监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc61/10377814/0c961afcb2e8/curroncol-30-00476-g001.jpg

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